173 Wet Analysis Jobs - Page 7

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-8 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ Inprocess / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. Perks & Benefits Dynamic work environment Career development opportuniti...

Walk-in Drive @ Ahmedabad on 18th May'25 (Sunday) for Quality Control Department We are looking for suitable candidates for OSD Quality Control for Ahmedabad location Unit Interview Venue Details: Date: 18th May 25 (Sunday), Time: - 9:00 AM to 1:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd Survey No. 634,637-641 Village: Rajoda Tal: Bavla Dist: Ahmedabad -Gujarat - 382220 1) REQUIREMENT FOR OSD QUALITY CONTROL DEPARTMENT Total Experience: 02 to 7 years (Pharma experience only) Qualification: B.Sc./ M.Sc/ B. Pharm/ M. Pharm Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Desired Profile: Test RM, PM, in-process, finished & stability samples (various do...

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Responsibilities: Conduct wet analyses and method validations Ensure compliance with industry standards and regulatory requirements Maintain cleanliness and safety protocols in the lab environment Share cvs to ramya_n@hikal.com

Designation - Chemist /Officer / Sr. Officer - QC Company - Leading Chemical Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. Experience - 1yr. to 6yrs. Total Openings - 5 Nos. share with your friends. Required Candidate profile Analysis of RM, PM, IP, FG prepare approved or rejected test report calibration activity for laboratory instrument like - GC, HPLC, IC, Balance, pH Meter, Ion Analyzer, Karl Fischer Total Openings- 5

Essential Skills: Should have knowledge & Experience for Sampling and Testing of Raw Material, Packaging Materials, Intermediates and Finished Products. Major Responsibilities 1) Should have Hands on Experience in Sampling and Chemical Testing of Raw Materials, Packaging Materials, Intermediates and Finished Products. 2) Should have basic knowledge of Volumetric Solution preprations and Standaradizations, Calibrations of Equipments and its required Documentation. 3) Should have knowledge of cGMP, GLP and GHP and should have Hands on Experience of SAP QA Module.

ob Title: Assistant Manager Quality Control Job Location - Bathinda/ Rajpura, Punjab Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide o...

Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & ex...

Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. po...

Role & responsibilities : 1) To plan analysis of in- process, intermediate, raw material, stability sample, holding time study sample & finished products on HPLC & check report of the same. (Dirty Equipment & Clean Equipment) 2) To distribute the shift wise work to analyst as per requirement in HPLC section & To plan calibration of HPLC /analytical balance as per schedule and review the same.

Role & responsibilities Analyze all raw materials and finished goods as per QC Manager instructions and SOPs. Follow analytical methods from the Development & Application department and USP test standards. Handle in-process quality control (IPC), outgoing quality control, and validation data. Represent QC & QA during audits and maintain records per regulatory requirements. Refuse or stop production when quality issues arise and inform concerned managers. Collect and retain product samples according to SOPs. Analyze online collection samples as per SOP. Ensure production operations comply with cGMP, ISO 15378, Maintain GMP compliance in the workplace and meet targeted production quality stand...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Job Details: Responsible for establishing the performance of R&D formulations for water treatment applications. Creating lab SOPs for different water treatment analysis methods. Supporting the field team by performing trial sample analysis in lab. Maintaining the lab equipment, analytical records, sample inventory. Training the underworking staff for routine lab work. 1. Job Responsibilities & Duties: a. Executing application trials for product development in the water lab across various stages of treatment. b. Planning for daily experiments. c. Reading research articles and contributes to the research d. Formulation development e. Collaborating with field team to run troubleshooting experim...

Roles and Responsibilities Conduct quality control tests on raw materials, in-process samples, finished products, and stability studies using HPLC, GC, UV, Dissolution, LIMS, Microbiology techniques. Ensure compliance with GLP guidelines for laboratory operations and maintain accurate records of test results. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and execute protocols for wet analysis testing of pharmaceutical products. Participate in audits conducted by regulatory authorities or internal stakeholders.

Oversees QC processes, ensuring products meet specified std. Developing and implementing QC procedures, conducting audits, and resolving qc-related issues. trains the QC team, maintains records, and ensures compliance with regulatory standards

Experience of FG/RM/Stability Analysis, validation samples and method validation . Must have handled HPLC ,GC,UV & other related QC instruments. Exposure of analysis in Formulations: Tablets/capsules

Responsibilities: Responsible for Documentation work in QC Department Candidate must have Experience of HPLC , GC & Wet Analysis. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing material. To ensure the compliance of safety Requirement Cleanliness Hygiene and Environment in Working Areas. Responsible for Domestic / Export/ batch production & their Documents for their smooth Dispatch Activity. Required Skills: Team player Good in communication Required Qualification: - B.Sc/M.Sc - Chemistry

Responsibilities: To follow Good Laboratory Practices. Carry out routine analysis & Ensure documents pertaining to day to day analysis. Calibrate instrument used for analysis as per SOP and maintain its record. Method Transfer Activity. Should have experience of handling and calibration of GC, HPLC, KF, UV, Viscometer, Potentiometer, Tintometer, PH Meter etc. Various analyticals methods development and wet analysis along with related documentation. Required Skills Must be excellent in written and spoken English; Net savvy and adept at computer skills. Good in communication. Required Qualification : - B.Sc/M.Sc - Chemistry

Role & responsibilities 1) Responsible for Laboratory execution of analytical activities on daily basis and ensuring compliance to the Safety and quality system as per cGMP. 2) Responsible for Laboratory execution of instrument calibration, stability analysis, WRS preparation/Qualification and for procurement of reference standard etc. 3) Responsible for maintaining stock of working reference standards and chemicals required routinely for raw material analysis. 4) Review and release of finished product, inprocess, intermediates, raw material, reaction monitoring results. 5) Responsible for Laboratory execution of analytical method validation/Verification and Method Transfer activites. 6) Coo...

Testing of Transformer Oil as per IS, IEC, ASTM and IEEE standards. Testing will be classified under Chemical, Physical and Electrical properties of the Transformer Oil. Handling the Instruments like GC and HPLC corresponding to the each testing parameters. Preparing required reagents corresponding to their testing parameters. Taking appropriate quality measures including preparation / maintenance of necessary documents and attending audits to ensure compliance with ISO 17025. Role & responsibilities Hardworking, Commitment and Continuously upgrading his/her knowledge and skills as per the requirement of the job. Ensuring proper quality control protocol and for taking necessary preventive an...

Role & responsibilities Sampling and analysis as per standard operating process Wear and ensure all helpers adhere to safety PPE s and follow safety standards. If discrepancy found in samples coordinate with Senior Chemist Take samples from inward vehicles and conduct Quick Check analysis Take in process sample for analysis and take corrective measures if not in coordination with Senior Chemist Check all instruments are in working condition and if not inform Senior Chemist Prepare all lab reagents and chemicals as per standards and discard if expired in coordination with Senior Chemist Implement Good House Keeping Practices and keep laboratory clean (5S) Instrument Handling COD- Digester, Ov...

Role & responsibilities Handling of Analytical Method validation of Assay and dissolution as per ICH Guidelines. Responsible for the Analysis of Finished products as per STP. Responsible for the Qualification and Maintenance of Working Standards. Responsible for sending of samples to external laboratory and receiving of reports. Maintenance of records / documents for external laboratory services. Dissolution: Carrying out different Media study with compilation of results. Regular Stability Analysis: Well versed with handling of regular Stability samples analysis. Operation and regular maintenance of stability chambers. Documentation: Good knowledge on GLP, GDP, CGMP and maintenance of record...

We are seeking a diligent and skilled QC Analyst to join our Quality Control Department. The ideal candidate will have hands-on experience in analytical techniques, a strong foundation in chemical analysis. Number : 9687066537